Yavuz Sevgi, Bayazıt Aysun Karabay, Anarat Ali, Gonlusen Gulfiliz, Alsancak Perihan
Division of Pediatric Nephrology, Cukurova University Hospital, Adana, Turkey.
Pediatr Int. 2015 Apr;57(2):310-3. doi: 10.1111/ped.12455.
Schimke immuno-osseous dysplasia (SIOD) is a rare hereditary disease characterized by skeletal dysplasia, immune deficiency and progressive renal disease. Kidney involvement mainly determines the prognosis. The most common renal pathology is focal segmental glomerulosclerosis (FSGS). Medullary nephrocalcinosis refers to the diffuse deposition of calcium salts in renal medulla and has not previously been identified in SIOD. Here we report the first case of a pediatric patient having typical features of SIOD with medullary nephrocalcinosis.
施姆克免疫性骨发育不良(SIOD)是一种罕见的遗传性疾病,其特征为骨骼发育不良、免疫缺陷和进行性肾脏疾病。肾脏受累情况主要决定预后。最常见的肾脏病理表现是局灶节段性肾小球硬化(FSGS)。髓质肾钙质沉着症是指钙盐在肾髓质的弥漫性沉积,此前在SIOD中尚未被发现。在此,我们报告首例具有SIOD典型特征并伴有髓质肾钙质沉着症的儿科患者。